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328062-46-0

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328062-46-0 Usage

Description

3-bromo-6-phenylimidazo[1,2-a]pyridine is a heterocyclic chemical compound with the molecular formula C12H8BrN3. It features both an imidazole and a pyridine ring, with a bromine atom at the 3-position and a phenyl group attached at the 6-position of the imidazo[1,2-a]pyridine ring. This halogenated derivative of imidazo[1,2-a]pyridine is utilized in organic synthesis and medicinal chemistry as a key building block for creating more complex molecules with potential biological activities. Due to its potential hazards and toxicity, careful handling of this compound is essential.

Uses

Used in Organic Synthesis:
3-bromo-6-phenylimidazo[1,2-a]pyridine is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows for further functionalization and modification, enabling the synthesis of a wide range of molecules with diverse properties and applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-bromo-6-phenylimidazo[1,2-a]pyridine is employed as a building block for the development of pharmaceuticals with potential therapeutic effects. Its incorporation into more complex molecular structures can lead to the discovery of new drugs with improved efficacy and selectivity.
Used in Drug Discovery:
3-bromo-6-phenylimidazo[1,2-a]pyridine is utilized in drug discovery processes as a starting point for the design and synthesis of novel bioactive molecules. Its structural features can be exploited to create compounds with specific binding affinities and selectivity towards biological targets, such as enzymes, receptors, or other proteins, which can be crucial for the treatment of various diseases.
Used in Chemical Research:
3-bromo-6-phenylimidazo[1,2-a]pyridine is also used in chemical research to study the properties and reactivity of heterocyclic systems. Understanding the behavior of 3-bromo-6-phenylimidazo[1,2-a]pyridine in different chemical reactions can provide valuable insights into the design of new synthetic routes and the development of innovative chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 328062-46-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,0,6 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 328062-46:
(8*3)+(7*2)+(6*8)+(5*0)+(4*6)+(3*2)+(2*4)+(1*6)=130
130 % 10 = 0
So 328062-46-0 is a valid CAS Registry Number.

328062-46-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-6-phenylimidazo[1,2-a]pyridine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:328062-46-0 SDS

328062-46-0Downstream Products

328062-46-0Relevant articles and documents

IMIDAZO[1,2-A]PYRIDINE AND PYRAZOLO[2,3-A]PYRIDINE DERIVATIVES

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Page/Page column 39, (2010/02/04)

A compound of formula (I) wherein Ring A is imidazol[1,2a]pyrid-3-yl or pyrazolo[2,3a]pyrid-3-yl; Ris as defined within; m is 0-5; wherein the values of Rmay be the same or different; Ris as defined within; n is 0 to 2, wherein the values of Rmay be the same or different; Ring B is phenyl or phenyl fused to a C5-7cycloalkyl ring; Ris as defined within; p is 0-4; wherein the values of Rmay be the same or different; Ris as defined within; q is 0-2; wherein the values of Rmay be the same or different; and wherein p+q=5; or a pharmaceutically acceptable salt or an in vivo hydrolyzable ester thereof is described. The use of compounds of formula (I) in the inhibition of cell cycle kinases CDK2, CDK4, and CDK6 are also described. Pharmaceutical compositions, methods and processes for preparation of compounds of formula (I) are detailed.

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